Variant (rsID / SNP)

rs2274987

rs2274987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SGIP1, DYNLT5. Location: chromosome 1, position 67,221,387. The table records no clinical significance for this variant.

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Reference-table entries

SGIP1Not classified

Variant type: downstream_gene_variant
Chromosome / position: 1:67221387
HGVS: NM_001350217.2,c.*12609T>C
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.